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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 19251 - 19275 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000192513b,7a,12a-Trihydroxy-5a-Cholanoic acid,2TMS,isomer#6JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C)C[C@@H]1C[C@H]3O[Si](C)(C)CTMS552.3666Semi standard non polar3336.1802
RI000192523b,7a,12a-Trihydroxy-5a-Cholanoic acid,3TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C)C[C@@H]1C[C@H]3OTMS624.4062Semi standard non polar3343.2441
RI000192533b,7a,12a-Trihydroxy-5a-Cholanoic acid,3TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O)C[C@@H]1C[C@H]3O[Si](C)(C)CTMS624.4062Semi standard non polar3329.1433
RI000192543b,7a,12a-Trihydroxy-5a-Cholanoic acid,3TMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C)C[C@@H]1C[C@H]3O[Si](C)(C)CTMS624.4062Semi standard non polar3321.5957
RI000192553b,7a,12a-Trihydroxy-5a-Cholanoic acid,3TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C)C[C@@H]1C[C@H]3O[Si](C)(C)CTMS624.4062Semi standard non polar3336.5137
RI000192563b,7a,12a-Trihydroxy-5a-Cholanoic acid,4TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C)C[C@@H]1C[C@H]3O[Si](C)(C)CTMS696.4457Semi standard non polar3341.1428
RI000192573b,7a,12a-Trihydroxy-5a-Cholanoic acid,1TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O)C[C@@H]1C[C@H]3OTBDMS522.3741Semi standard non polar3642.7913
RI000192583b,7a,12a-Trihydroxy-5a-Cholanoic acid,1TBDMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O)C[C@@H]1C[C@H]3OTBDMS522.3741Semi standard non polar3636.382
RI000192593b,7a,12a-Trihydroxy-5a-Cholanoic acid,1TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O)C[C@@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS522.3741Semi standard non polar3578.9707
RI000192603b,7a,12a-Trihydroxy-5a-Cholanoic acid,1TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C[C@H]3OTBDMS522.3741Semi standard non polar3656.7664
RI000192613b,7a,12a-Trihydroxy-5a-Cholanoic acid,2TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O)C[C@@H]1C[C@H]3OTBDMS636.4605Semi standard non polar3838.8474
RI000192623b,7a,12a-Trihydroxy-5a-Cholanoic acid,2TBDMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C[C@H]3OTBDMS636.4605Semi standard non polar3849.5317
RI000192633b,7a,12a-Trihydroxy-5a-Cholanoic acid,2TBDMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O)C[C@@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS636.4605Semi standard non polar3752.9692
RI000192643b,7a,12a-Trihydroxy-5a-Cholanoic acid,2TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C[C@H]3OTBDMS636.4605Semi standard non polar3798.591
RI000192653b,7a,12a-Trihydroxy-5a-Cholanoic acid,2TBDMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O)C[C@@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS636.4605Semi standard non polar3767.2058
RI000192663b,7a,12a-Trihydroxy-5a-Cholanoic acid,2TBDMS,isomer#6JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS636.4605Semi standard non polar3761.418
RI000192673b,7a,12a-Trihydroxy-5a-Cholanoic acid,3TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C[C@H]3OTBDMS750.547Semi standard non polar3986.646
RI000192683b,7a,12a-Trihydroxy-5a-Cholanoic acid,3TBDMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O)C[C@@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS750.547Semi standard non polar3958.4512
RI000192693b,7a,12a-Trihydroxy-5a-Cholanoic acid,3TBDMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS750.547Semi standard non polar3941.7725
RI000192703b,7a,12a-Trihydroxy-5a-Cholanoic acid,3TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS750.547Semi standard non polar3967.2468
RI000192713b,7a,12a-Trihydroxy-5a-Cholanoic acid,4TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS864.6335Semi standard non polar4162.0063
RI000192723b,7a,12a-Trihydroxy-5a-Cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)C[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized408.2876Standard polar4216.655
RI000192733b,7a,12a-Trihydroxy-5a-Cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)C[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized408.2876Standard non polar3464.1238
RI000192743b,7a,12a-Trihydroxy-5a-Cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)C[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized408.2876Semi standard non polar3681.9438
RI000192753a,6b,7b,12b-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1[C@H](O)[C@@H]3OTMS496.322Semi standard non polar3481.1973
Displaying retention index compounds 19251 - 19275 of 1722868 in total